| glyA基因的克隆及其在毕赤酵母中的表达 |
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| 引用本文： | 王博,祝林,马立新.glyA基因的克隆及其在毕赤酵母中的表达[J].氨基酸和生物资源,2006,28(2):45-47. |
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| 作者姓名： | 王博 祝林 马立新 |
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| 作者单位： | 湖北大学生命科学学院分子微生物与基因工程实验室,湖北大学,武汉,430062 |
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| 摘 要： | 根据已知的序列设计引物,以大肠杆菌XL10-Gold总DNA为模板进行梯度PCR,并进行DNA序列测定,其序列与已经报道的glyA基因完全一致。将其克隆到毕赤酵母分泌型表达载体pHBM905C上,获得表达质粒pHBM1001.该质粒转化毕赤酵母GS115所得重组子经PCR验证后成功进行了诱导表达,并初步测定了酶活力。
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| 关 键 词： | glyA基因 毕赤酵母 基因克隆 分泌表达 |
| 文章编号： | 1006-8376(2006)02-0045-03 |
| 收稿时间： | 02 14 2006 12:00AM |
| 修稿时间： | 2006年2月14日 |
Cloning of glyA Gene and Its Expression in Pichia pastoris |
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| WANG Bo,ZHU Lin,MA Li-xin.Cloning of glyA Gene and Its Expression in Pichia pastoris[J].Amino Acids & Biotic Resources,2006,28(2):45-47. |
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| Authors: | WANG Bo ZHU Lin MA Li-xin |
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| Abstract: | Based on the published sequence,a DNA fragment was cloned by touchdown PCR from E.coli XL10-Gold.Sequencing showed that this fragment was the same as the published glyA gene.This fragment was inserted into the Pichia pastoris excretion expression vector pHBM905C,and pHBM1001 was obtained.Then the pHBM1001 was introduced into Pichia pastoris GS115,and one clone was selected for induced expression after PCR confirmation,SHMT activity also was obtained. |
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| Keywords: | glyA gene Pichia pastoris gene cloning excretion expression |
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